SNTG2 antibody (AA 181-280)

Catalog No. ABIN1385151

This anti-SNTG2 antibody is a Rabbit Polyclonal antibody detecting SNTG2 in WB, IF (cc), IF (p), ELISA, IHC (fro), IHC (p) and ICC. Suitable for Human.

Quick Overview for SNTG2 antibody (AA 181-280) (ABIN1385151)

Target: SNTG2 (Syntrophin, gamma 2 (SNTG2))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This SNTG2 antibody is un-conjugated

Application: Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), ELISA, Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunocytochemistry (ICC)

Product Details anti-SNTG2 Antibody

Binding Specificity: AA 181-280

Predicted Reactivity: Human,Mouse,Rat

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human SNTG2

Isotype: IgG

Application Details

Application Notes: WB 1:300-5000
ELISA 1:500-1000
IHC-P 1:200-400
IHC-F 1:100-500
IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200
ICC 1:100-500

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 μg/μL

Buffer: 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.

Preservative: ProClin

Precaution of Use: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

Storage: 4 °C,-20 °C

Storage Comment: Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.

Expiry Date: 12 months

Target Details for SNTG2

Target: SNTG2 (Syntrophin, gamma 2 (SNTG2))

Alternative Name: SNTG2/Syntrophin 5

Background:

Synonyms: G2SYN, Gamma2-syntrophin, SNTG2, SYN5, Syntrophin-5, Syntrophin5, Syntrophin 5, Syntrophin gamma 2, SNTG2_HUMAN.

Background: Syntrophins are cytoplasmic peripheral membrane proteins that bind to components of mechanosenstive sodium channels and the extreme carboxy-terminal domain of dystrophin and dystrophin-related proteins. The PDZ domain of this protein product interacts with a protein component of a mechanosensitive sodium channel that affects channel gating. Absence or reduction of this protein product has been associated with Duchenne muscular dystrophy.